Treatment of Ocular Surface Disease in Ocular Cicatricial Pemphigoid.

IF 2.6 4区 医学 Q2 OPHTHALMOLOGY Ocular Immunology and Inflammation Pub Date : 2024-10-09 DOI:10.1080/09273948.2024.2413892
Kaleb S Abbott, Alan G Palestine, Scott G Hauswirth, Darren G Gregory, Jennifer L Patnaik, Amit K Reddy
{"title":"Treatment of Ocular Surface Disease in Ocular Cicatricial Pemphigoid.","authors":"Kaleb S Abbott, Alan G Palestine, Scott G Hauswirth, Darren G Gregory, Jennifer L Patnaik, Amit K Reddy","doi":"10.1080/09273948.2024.2413892","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>While substantial research has focused on systemic immunomodulatory therapy for ocular cicatricial pemphigoid (OCP), limited data exist on managing associated ocular surface disease (OSD). This study evaluates treatments for OCP-related OSD at our institution.</p><p><strong>Methods: </strong>We conducted a retrospective analysis of patients diagnosed with cicatrizing conjunctivitis at the University of Colorado Hospital from January 1, 2013, to October 31, 2023. Patients with cicatrizing conjunctivitis due to non-OCP conditions were excluded, and disease severity was classified using the Foster Staging System.</p><p><strong>Results: </strong>Our review included 30 patients with OCP, all with at least six months of follow-up. The mean age of symptom onset (<i>n</i> = 19) was 62.2 years (SD = 16.4), while the mean age at diagnosis (<i>n</i> = 28) was 65.1 years (SD = 12.7). The most common OSD treatments at the last visit were preservative-free artificial tears (87%), topical corticosteroids (43%), autologous serum eye drops (40%), topical antibiotics (30%), and topical immunomodulators (23%). All patients used at least one treatment, with 83.3% on prescription therapies. Patients averaged 3.33 (SD: 1.4) treatments, with 1.7 (SD: 1.2) being prescriptions. Topical immunomodulators had the highest discontinuation rate at 73.1% (<i>n</i> = 19/26). Autologous serum eye drops and topical corticosteroids were the least discontinued treatments. Number of total treatments, prescriptions, and procedures sharply increased at stage three OCP.</p><p><strong>Conclusions: </strong>The number of treatments and procedures increased with OCP severity, indicating that advanced OCP often necessitated more intensive OSD management.</p>","PeriodicalId":19406,"journal":{"name":"Ocular Immunology and Inflammation","volume":" ","pages":"1-7"},"PeriodicalIF":2.6000,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ocular Immunology and Inflammation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/09273948.2024.2413892","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: While substantial research has focused on systemic immunomodulatory therapy for ocular cicatricial pemphigoid (OCP), limited data exist on managing associated ocular surface disease (OSD). This study evaluates treatments for OCP-related OSD at our institution.

Methods: We conducted a retrospective analysis of patients diagnosed with cicatrizing conjunctivitis at the University of Colorado Hospital from January 1, 2013, to October 31, 2023. Patients with cicatrizing conjunctivitis due to non-OCP conditions were excluded, and disease severity was classified using the Foster Staging System.

Results: Our review included 30 patients with OCP, all with at least six months of follow-up. The mean age of symptom onset (n = 19) was 62.2 years (SD = 16.4), while the mean age at diagnosis (n = 28) was 65.1 years (SD = 12.7). The most common OSD treatments at the last visit were preservative-free artificial tears (87%), topical corticosteroids (43%), autologous serum eye drops (40%), topical antibiotics (30%), and topical immunomodulators (23%). All patients used at least one treatment, with 83.3% on prescription therapies. Patients averaged 3.33 (SD: 1.4) treatments, with 1.7 (SD: 1.2) being prescriptions. Topical immunomodulators had the highest discontinuation rate at 73.1% (n = 19/26). Autologous serum eye drops and topical corticosteroids were the least discontinued treatments. Number of total treatments, prescriptions, and procedures sharply increased at stage three OCP.

Conclusions: The number of treatments and procedures increased with OCP severity, indicating that advanced OCP often necessitated more intensive OSD management.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
治疗眼部角化性丘疹病的眼表疾病。
目的:虽然大量研究都集中在眼部卡他性丘疹病(OCP)的全身免疫调节疗法上,但关于治疗相关眼表疾病(OSD)的数据却很有限。本研究评估了我院对 OCP 相关 OSD 的治疗方法:我们对科罗拉多大学医院从 2013 年 1 月 1 日至 2023 年 10 月 31 日确诊的卡他性结膜炎患者进行了回顾性分析。我们排除了非 OCP 引起的卡他性结膜炎患者,并使用福斯特分期系统对疾病严重程度进行了分类:我们的研究共纳入了 30 名 OCP 患者,所有患者均接受了至少 6 个月的随访。平均发病年龄(n = 19)为 62.2 岁(SD = 16.4),平均确诊年龄(n = 28)为 65.1 岁(SD = 12.7)。上次就诊时最常用的 OSD 治疗方法是不含防腐剂的人工泪液(87%)、局部皮质类固醇(43%)、自体血清滴眼液(40%)、局部抗生素(30%)和局部免疫调节剂(23%)。所有患者都使用了至少一种治疗方法,其中 83.3% 使用处方疗法。患者平均使用 3.33 种(标度:1.4)疗法,其中 1.7 种(标度:1.2)为处方疗法。局部免疫调节剂的停药率最高,达到 73.1%(n = 19/26)。自体血清滴眼液和外用皮质类固醇是停用率最低的治疗方法。在 OCP 第三阶段,总治疗次数、处方和手术次数急剧增加:结论:治疗次数和手术次数随着 OCP 严重程度的增加而增加,这表明晚期 OCP 通常需要更密集的 OSD 管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.20
自引率
15.20%
发文量
285
审稿时长
6-12 weeks
期刊介绍: Ocular Immunology & Inflammation ranks 18 out of 59 in the Ophthalmology Category.Ocular Immunology and Inflammation is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and vision scientists. Published bimonthly, the journal provides an international medium for basic and clinical research reports on the ocular inflammatory response and its control by the immune system. The journal publishes original research papers, case reports, reviews, letters to the editor, meeting abstracts, and invited editorials.
期刊最新文献
Multimodal Imaging in Unilateral Acute Idiopathic Maculopathy with Staphylococcus aureus Infection. Bilateral Involvement in Childhood Presumed Trematode Induced Granulomatous Anterior Uveitis. MicroRNAs as Biomarkers for Uveitis in Juvenile Idiopathic Arthritis. Is it Time to Adopt a New Nomenclature and Classification for White Dot Syndromes Using Multimodal Imaging Techniques? Report 1 from Multimodal Imaging in Uveitis (MUV) Task Force. Vogt-Koyanagi-Harada Disease Presenting as Papillitis vs. Classic Serous Retinal Detachment: A Comparative Analysis of Outcomes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1